Muonium atoms observed in liquid hydrocarbons

1980 ◽  
Vol 58 (23) ◽  
pp. 2395-2401 ◽  
Author(s):  
Yasuo Ito ◽  
Bill W. Ng ◽  
Yan-Ching Jean ◽  
David C. Walker

Muonium atoms have been observed in n-hexane, c-hexane, and tetramethylsilane at 295 or 273 K by the MSR technique. The yield of muonium in these non-polar liquids is found to be quite comparable to that observed previously in water, methanol, and ethanol. This suggests that neither the dielectric constant of the medium nor the free-electron mobility has a major influence on the formation process. This in turn supports the view that muonium formation does not mainly result from intraspur reactions in the terminal spur of the muon's track.The chemical lifetime of muonium in these hydrocarbons is curtailed by spurious impurities so that high purity is required. In addition, however, there may be a chemical reaction between muonium and the hydrocarbon itself because the maximum lifetime found increases in the order of increasing bond energy. Reaction rate constants with added solutes have also been measured, and these observations open up the possibility of studying hydrophobic solutes and extending hydrogen-isotope studies to biologically-important media.

2010 ◽  
Vol 114 (4) ◽  
pp. 1783-1789 ◽  
Author(s):  
S. Jason Dee ◽  
Vanessa A. Castleberry ◽  
Otsmar J. Villarroel ◽  
Ivanna E. Laboren ◽  
Darrin J. Bellert

Author(s):  
M.A. Egyan ◽  

The article shows studies characterizing the quality of the squeeze: the mechanical composition of the squeeze is determined, the structural moisture of each component is determined, the sugar content in the formed process of sedimentation of the juice and its acidity are determined refractometrically. The kinetics of anthocyanins extraction was determined in two ways, the solids content in the extract was calculated, and the reaction rate constants of the extraction process and the efficiency coefficient of ultrasonic amplification of the extraction process speed were calculated.


Author(s):  
Daria S. Timofeeva ◽  
David M Lindsay ◽  
W. J. Kerr ◽  
David James Nelson

Herein we examine the relationship between reaction rate and reaction selectivity in iridium-catalysed hydrogen isotope exchange (HIE) reactions directed by Lewis basic functional groups. We have recently develped a directing...


1999 ◽  
Vol 103 (15) ◽  
pp. 2664-2672 ◽  
Author(s):  
Kazuaki Tokuhashi ◽  
Hidekazu Nagai ◽  
Akifumi Takahashi ◽  
Masahiro Kaise ◽  
Shigeo Kondo ◽  
...  

2014 ◽  
Vol 59 (1) ◽  
pp. 2252-2259 ◽  
Author(s):  
ZHEN CHEN ◽  
XINLIANG YU ◽  
XIANWEI HUANG ◽  
SHIHUA ZHANG

1989 ◽  
Vol 67 (5) ◽  
pp. 857-861 ◽  
Author(s):  
Shin-Ichi Miyamoto ◽  
Tetsuo Sakka ◽  
Matae Iwasaki

The reaction rate of hydrogen isotope exchange between D2 and H2O catalyzed by platinum plate is studied. The exchange reaction is described with the kinetic model which is the modification of that for the exchange reaction catalyzed by alumina-supported platinum catalyst. For the comparison of experimental results with this model relative amount of the number of sites for hydrogen adsorption was estimated from the initial rate of hydrogen isotope exchange between H2 and D2 on the same surface. The results show that the kinetic model is applicable for the plate catalyst if the number of the sites for hydrogen absorption, which is very sensitive to the surface state of the catalyst, was estimated not from the macroscopic surface area but from our scheme. Keywords: hydrogen isotope exchange reaction, platinum plate as catalyst.


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